Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia. (Q50874132)

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scientific article published in May 1998

Language	Label	Description	Also known as
English	Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia.	scientific article published in May 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia. (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

1 reference

based on heuristic

inferred from title

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based on heuristic

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object named as

Boomsma DI

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Europe PubMed Central

PubMed publication ID

24 March 2018

author name string

Hoffer MJ

1

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Bredie SJ

2

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Snieder H

3

1 reference

Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Reymer PW

4

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Demacker PN

5

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Havekes LM

6

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Stalenhoef AF

8

1 reference

Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Frants RR

9

1 reference

Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Kastelein JJ

10

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

publication date

1 May 1998

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Atherosclerosis

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

138

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24 March 2018

http://europepmc.org/abstract/MED/9678774

1

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PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

91-99

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Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

1 reference

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7 January 2021

Inheritance of combined hyperlipoproteinemia: evidence for a new lipoprotein phenotype.

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7 January 2021

Hyperapobetalipoproteinemia in a kindred with familial combined hyperlipidemia and familial hypercholesterolemia

1 reference

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7 January 2021

Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia

1 reference

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7 January 2021

Structure of the human lipoprotein lipase gene

1 reference

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7 January 2021

Human genes involved in lipolysis of plasma lipoproteins: mapping of loci for lipoprotein lipase to 8p22 and hepatic lipase to 15q21

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7 January 2021

Human lipoprotein lipase complementary DNA sequence.

1 reference

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7 January 2021

Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.

1 reference

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7 January 2021

Detection and characterization of the heterozygote state for lipoprotein lipase deficiency

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7 January 2021

Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation

1 reference

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7 January 2021

DNA polymorphisms at the lipoprotein lipase gene: associations in normal and hypertriglyceridaemic subjects.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

A common variant in the gene for lipoprotein lipase (Asp9-->Asn). Functional implications and prevalence in normal and hyperlipidemic subjects.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Comparison of gemfibrozil versus simvastatin in familial combined hyperlipidemia and effects on apolipoprotein-B-containing lipoproteins, low-density lipoprotein subfraction profile, and low-density lipoprotein oxidizability

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Extensions to pedigree analysis. III. Variance components by the scoring method

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic males

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

A common mutation in the lipoprotein lipase gene promoter, -93T/G, is associated with lower plasma triglyceride levels and increased promoter activity in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Family study of lipoprotein lipase gene polymorphisms and plasma triglyceride levels

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

A hepatic lipase (LIPC) allele associated with high plasma concentrations of high density lipoprotein cholesterol

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Association between the LPL-D9N mutation in the lipoprotein lipase gene and plasma lipid traits in myocardial infarction survivors from the ECTIM study

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

The Asp9 Asn mutation in the lipoprotein lipase gene is associated with increased progression of coronary atherosclerosis. REGRESS Study Group, Interuniversity Cardiology Institute, Utrecht, The Netherlands. Regression Growth Evaluation Statin Study

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia.

1 reference

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7 January 2021

No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

Familial combined hyperlipidemia and abnormal lipoprotein lipase

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900007-0

7 January 2021

based on heuristic

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Identifiers

10.1016/S0021-9150(98)00007-0

1 reference

Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 March 2018

http://europepmc.org/abstract/MED/9678774

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